首页> 外文期刊>Scandinavian journal of infectious diseases. >Lack of association of outcomes with treatment duration and microbiologic susceptibility data in Clostridium difficile infections in a non-NAP1/BI/027 setting
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Lack of association of outcomes with treatment duration and microbiologic susceptibility data in Clostridium difficile infections in a non-NAP1/BI/027 setting

机译:在非NAP1 / BI / 027环境中,艰难梭菌感染的治疗结果与治疗持续时间和微生物敏感性数据缺乏关联

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Background: Concerns regarding the poor response of severe Clostridium difficile infection (CDI) treated with metronidazole have arisen over the last 5 y. Methods: We conducted a prospective, non-interventional study of CDI cases at our institution to evaluate the role of drug resistance, co-morbidities, and the emergence of hypervirulent strains on patient outcomes. A total of 118 adult inpatients with diarrhea and a positive stool for C. difficile toxin immunoassay had positive stool cultures and were included in the study. All 118 isolates had vancomycin and metronidazole susceptibility testing via the E-test method; rep-PCR was performed on 47 isolates. Of the 118 study patients, 107 were treated with either metronidazole or vancomycin. Results: Initial therapy was metronidazole in 98.1% (n = 105) and vancomycin in 1.9% (n = 2) patients. Evaluable clinical response within 5 days of treatment was noted in 52.5% (52/99) of cases. The mean duration of treatment was 11.7 ± 7.2 days. The 30-day all-cause mortality rate was 24.6% (29/118). Recurrence occurred in 23.6% (21/89). A recent stay in the intensive care unit was associated with increased 30-day mortality (odds ratio 3.58, p = 0.012). There were no isolates resistant to metronidazole or vancomycin. Only 1 isolate was possibly related to the NAP1/BI/027 reference strain. No strain-related differences in deaths or recurrence were noted. Conclusions: Deaths related to CDI in our study appear to be related to multiple factors and did not appear to be independently related to antibiotic susceptibility, strain type, or treatment duration.
机译:背景:在过去的5年中,出现了对用甲硝唑治疗的严重艰难梭菌感染(CDI)反应差的担忧。方法:我们在我们的机构中​​对CDI病例进行了一项前瞻性,非干预性研究,以评估耐药性,合并症和高毒力菌株的出现对患者预后的作用。共有118名成年腹泻住院患者和艰难梭菌毒素免疫测定粪便阳性,粪便培养阳性,被纳入研究。所有118株分离株均通过E-test法进行了万古霉素和甲硝唑敏感性测试。对47个分离株进行rep-PCR。在118位研究患者中,有107位接受了甲硝唑或万古霉素治疗。结果:初始治疗为甲硝唑98.1%(n = 105)和万古霉素1.9%(n = 2)患者。 52.5%(52/99)的病例在治疗5天内可评估的临床反应。平均治疗时间为11.7±7.2天。 30天全因死亡率为24.6%(29/118)。复发发生率为23.6%(21/89)。最近在重症监护病房的住院与30天死亡率增加有关(赔率3.58,p = 0.012)。没有对甲硝唑或万古霉素有抗药性的菌株。只有1个分离物可能与NAP1 / BI / 027参考菌株有关。没有发现与菌株相关的死亡或复发差异。结论:在我们的研究中,与CDI相关的死亡似乎与多种因素有关,与抗生素的敏感性,菌株类型或治疗时间无关。

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